Effects of adhesions of amorphous Fe and Al hydroxides on surface charge and adsorption of K+ and Cd2+ on rice roots

被引:15
作者
Liu, Zhao-dong [1 ,2 ]
Wang, Hai-cui [1 ,2 ]
Zhou, Qin [1 ,2 ]
Xu, Ren-kou [1 ]
机构
[1] Chinese Acad Sci, Inst Soil Sci, State Key Lab Soil & Sustainable Agr, POB 821, Nanjing, Jiangsu, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Al hydroxide; Fe hydroxide; Rice roots; Surface charge; Zeta potential; Potassium and cadmium adsorption; CATION-EXCHANGE CAPACITY; ORYZA-SATIVA L; ELECTRICAL POTENTIALS; IRON PLAQUE; CELL-WALLS; ION INTERACTIONS; PROTON BINDING; METAL UPTAKE; FT-IR; SOILS;
D O I
10.1016/j.ecoenv.2017.07.033
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Iron (Fe) and aluminum (Al) hydroxides in variable charge soils attached to rice roots may affect surface-charge properties and subsequently the adsorption and uptake of nutrients and toxic metals by the roots. Adhesion of amorphous Fe and Al hydroxides onto rice roots and their effects on zeta potential of roots and adsorption of potassium (K+) and cadmium (Cd2+) by roots were investigated. Rice roots adsorbed more Al hydroxide than Fe hydroxide because of the greater positive charge on Al hydroxide. Adhesion of Fe and Al hydroxides decreased the negative charge on rice roots, and a greater effect of the Al hydroxide. Consequently, adhesion of Fe and Al hydroxides reduced the K+ and Cd2+ adsorption by rice roots. The results of attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR) and desorption of K+ and Cd2+ from rice roots indicated that physical masking by Fe and Al hydroxides and diffuse-layer overlapping between the positively-charged hydroxides and negatively-charged roots were responsible for the reduction of negative charge on roots induced by adhesion of the hydroxides. Therefore, the interaction between Fe and Al hydroxides and rice roots reduced negative charge on roots and thus inhibited their adsorption of nutrient and toxic cations.
引用
收藏
页码:207 / 213
页数:7
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